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作 者:薛金教[1] 顾冉冉[1] 袁英歌[1] 游义霞[1] 彭明[1] 崔百明[1]
机构地区:[1]石河子大学农业生物技术重点实验室/石河子大学生命科学学院,石河子832003
出 处:《石河子大学学报(自然科学版)》2010年第3期265-269,共5页Journal of Shihezi University(Natural Science)
基 金:国家转基因重大专项项目(2008ZX08005-002);国家自然科学基金项目(307600991)
摘 要:为了扩展可再生棉花的基因型,选取新疆自育海岛棉品种新海15的胚珠为外植体,利用组织培养的方法进行再生体系的建立。结果表明:含0.5mg/L KT和0.5mg/L 2,4-D的MSB培养基,在暗培养条件下可诱导胚珠,产生初始愈伤;愈伤分化则以含0.05/0.1mg/L KT和0.1mg/L 2,4-D的MSB培养基效果较佳;选取浅黄色、结构疏松的愈伤组织在含较高浓度IBA和较低浓度KT、2,4-D的3种调控培养基上依次继代,以此实现胚性愈伤组织的增殖及细胞状态调控;液体悬浮培养和干燥胁迫处理均有利于胚性愈伤的体细胞胚胎诱导;子叶胚的萌发及植株再生则以含谷氨酰胺和天冬酰胺的1/2 MSB培养基效果较佳。Ovule of Xinhai 15,a breed of Gossypium barbadense cultured in Xinjiang,were used as explant to figure out a favorable culture system for the regeneration of somatic embryo.The result indicates that Calli of ovule were effectively produced on the medium with 0.5mg/L Kinetin(KT) and 0.5mgL 2,4-Dichlorophenoxyacetic acid(2,4-D) in darkness.The best culture media for callus differentiation is MSB media supplemented with 0.05/0.1mg/L KT and 0.1mg/L 2,4-D.To produce embryogenic calli and control the cell statue,light yellow,loose callus were cultured on three different control medias supplemented with high concentration of IBA and low concentration of KT and 2,4-D one after another.Liquid suspend and dehydration are beneficial to the emergence of somatic embryo.Plantlets were effectively regenerated on the 1/2 MSB media supplemented with L-Glutamine and L-Asparagine.
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